Phenotypes for disease #00853 (AOA3 (ataxia-oculomotor apraxia, type 3 (AOA-3)), OMIM:615217)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000093276 truncal ataxia with impaired ocular movement, elevated alpha-fetoprotein levels - - Familial, autosomal recessive - - 14y - - Nada Al Tassan 00117895
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